Spermatogenic defects in F2 mice between normal mouse strains C3H and C57BL/6 without mutation

Congenit Anom (Kyoto). 2012 Dec;52(4):186-90. doi: 10.1111/j.1741-4520.2012.00379.x.

Abstract

Genetic disorders are usually considered to be caused by harmful gene mutations, as well as by chromosomal aberrations, including small insertions, duplications and/or deletions. However, as infertile individuals often arise among the offspring of crosses between two fertile mouse strains, we postulate that a certain combination of 'normal' genes with neither gene mutations nor chromosomal aberrations can cause such serious phenotypic alterations as reproductive dysfunction. In this study, we show evidence that a combination of multiple normal genes from two different normal mouse strains manifests a wide range of male reproductive dysfunctions, from benign changes to complete infertility. These abnormal phenotypes are thought to have occurred by epistatic interactions of alleles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Crosses, Genetic
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Multifactorial Inheritance / genetics
  • Mutation*
  • Phenotype*
  • Sperm Head / pathology
  • Spermatogenesis / genetics*
  • Spermatozoa / pathology
  • Testis / pathology